Canonical Allele Identifier: CA232593089

Gene: ZNF705A

Linked Data

• dbSNP Id: rs989986234
• gnomAD v3: 12-8138662-A-G
• gnomAD v4: 12-8138662-A-G
• MyVariant Identifiers: chr12:g.8291258A>G (hg19) ; chr12:g.8138662A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8138662A>G , CM000674.2:g.8138662A>G	GRCh38
NC_000012.11:g.8291258A>G , CM000674.1:g.8291258A>G	GRCh37
NC_000012.10:g.8182525A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000402465.8:c.114+409A>G
ENST00000402465.7:c.-151+409A>G	ENSP00000384896.3:n.-151+409A>G